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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585337Generated: October 29, 2026

Toluene → HCID 69933131, compound

https://huagongshe.com/reaction/585337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl vinyl etherHCID 8023—
ReactantSodium CarbonateHCID 10340—
Reactant[2-Bromo-5-(hydroxymethyl)phenyl]methanolHCID 12968884—
Reactant(2-Bromo-1,3-phenylene)dimethanolHCID 15468755—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
ProductHCID 69933131HCID 6993313197.1%

Reaction Steps

To a suspension obtained by dispersing an about 93:7 mixture (22.1 g) of 2,4-bis(hydroxymethyl)bromobenzene and 2,6-bis(hydroxymethyl)bromobenzene, and p-toluenesulfonic acid monohydrate (0.1 g) in toluene (220 ml) was added dropwise ethyl vinyl ether (18.4 g) at 24-32° C., and the mixture was stirred at room temperature for 2 hr. The reaction mixture was poured into 5% aqueous sodium carbonate solution (100 ml), and the organic layer was washed with 5% aqueous sodium carbonate solution (100 ml), and dried over potassium carbonate. The solvent was evaporated to give an about 93:7 mixture (35.7 g, 97.1%) of 2,4-bis(1′-ethoxyethoxymethyl)bromobenzene and 2,6-bis(1′-ethoxyethoxymethyl)bromobenzene as a yellow oil. 2,4-bis(1′-Ethoxyethoxymethyl)bromobenzene was isolated by preparative HPLC and used in the measurement.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930211B2
Source datasetuspto-grants-2005_08
ORD IDord-5dfc70a4a08f4c4fa20d9bbd201dca06
Source noteuspto-grants-2005_08